Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor

Cancer Genet Cytogenet. 1991 May;53(1):91-5. doi: 10.1016/0165-4608(91)90118-e.

Abstract

We report three new cases with a hematologic disorder and the unbalanced translocation der(1)t(1;7)(p11;p11). It has been speculated that the gene for the epidermal growth factor receptor, localized to the short arm of chromosome 7, might be amplified in cases with this translocation. We have demonstrated that there is no amplification of this gene in these three cases.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 7*
  • ErbB Receptors / genetics*
  • Female
  • Gene Amplification*
  • Hematologic Diseases / genetics*
  • Humans
  • Male
  • Middle Aged
  • Multiple Myeloma / genetics
  • Polycythemia Vera / genetics
  • Primary Myelofibrosis / genetics
  • Translocation, Genetic*

Substances

  • ErbB Receptors